Classifications

• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/1601—Process or apparatus
  • C23C18/1633—Process of electroless plating
  • C23C18/1635—Composition of the substrate
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/1601—Process or apparatus
  • C23C18/1633—Process of electroless plating
  • C23C18/1635—Composition of the substrate
  • C23C18/1639—Substrates other than metallic, e.g. inorganic or organic or non-conductive
  • C23C18/1641—Organic substrates, e.g. resin, plastic
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/1601—Process or apparatus
  • C23C18/1633—Process of electroless plating
  • C23C18/1646—Characteristics of the product obtained
  • C23C18/165—Multilayered product
  • C23C18/1653—Two or more layers with at least one layer obtained by electroless plating and one layer obtained by electroplating
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/18—Pretreatment of the material to be coated
  • C23C18/20—Pretreatment of the material to be coated of organic surfaces, e.g. resins
  • C23C18/22—Roughening, e.g. by etching
  • C23C18/24—Roughening, e.g. by etching using acid aqueous solutions
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
  • D06M11/83—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with metals; with metal-generating compounds, e.g. metal carbonyls; Reduction of metal compounds on textiles
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/1601—Process or apparatus
  • C23C18/1633—Process of electroless plating
  • C23C18/1655—Process features
  • C23C18/1658—Process features with two steps starting with metal deposition followed by addition of reducing agent
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/18—Pretreatment of the material to be coated
  • C23C18/20—Pretreatment of the material to be coated of organic surfaces, e.g. resins
  • C23C18/28—Sensitising or activating
  • C23C18/30—Activating or accelerating or sensitising with palladium or other noble metal

Definitions

• This invention relates to a process for making completely and substantially uniformly metal coated polymeric monofilaments or yarn made from a plurality of such polymeric monofilaments which are coated with electrolessly deposited nickel and optionally with electrolytically deposited metal on the nickel. More particularly, this invention relates to a process for activating the surfaces of polymeric monofilaments which are subsequently coated with electrolessly deposited nickel.
• yam of monofilaments to be treated is unwound from a feed storage reel, passed through the appropriate chemical treating steps and then stored on a take up reel.
• the monofilaments positioned within the interior of the yam are not coated or are insufficiently coated so that the metal coatings on the monofilaments are non-uniform.
• a non-uniformly coated yam has undesirable nonuniform electrical conductivity. In many applications, such as for protective outside layers for cables, non-uniform metal outside layers are unacceptable.
• electroless nickel has been extremely difficult to deposit electroless nickel uniformly and completely onto the surface of monofilaments in a multifilament yarn bundle by wet chemical electroless processes.
• Various types of pre- woven fabric are coated with electroless metal, primarily electroless copper, for use as electromagnetic interference (EMI) control and shielding.
• electroless copper although appearing to have adequate adhesion to the individual monofilament polymer surface in a pre-woven fabric, for reasons not entirely understood, will not maintain its adhesion after exposure to high temperature or humidity exposure.
• This problem can be alleviated by using electroless nickel which forms tight polymeric bonds to the various functional groups on the surface of polymers which have been treated by the process of this invention.
• the resultant nickel-coated filaments are resistant to degradation exposure to thermal cycling and humidity.
• U.S. Patent 5,302,415 describes a process for electrolessly metalizing various aramid fibers using copper, nickel, silver, or cobalt.
• the disclosed process utilizes an 80 to 90% sulfuric acid solution to modify the surfaces of the aramid fibers. Modification is achieved by controlled fiber degradation as a consequence of depolymerization, to provide sites for the deposition of a sensitizer which promotes electroless metal deposition.
• the aramid fibers cannot be contacted with this strong sulfuric acid solution for more than a short time period because the fibers will dissolve or be degraded in the acid.
• electroless copper typically produces a coarse-grained coating which lacks the adhesion, ductility and flexural endurance that cable shielding applications in question require. Furthermore, an all-electroless copper construction requires the addition of another metal layer on each monofilament to protect the exposed copper against long-term oxidation.
• Nickel deposition by conventional phosphite-reduced electroless nickel processes results in a coating with a conductivity typically less than 15% that of copper. Due to oxidation of the phosphorous in the nickel-phosphorous alloy, of those nickel processes, such coatings form a much more stable surface and are generally preferred for applications involving high corrosion resistance. However, they are highly resistive and difficult to clean.
• the present invention provides a process for modifying the surface 10 of a polymeric monofilament to render said surface water- wettable characterized by contacting said surface with an aqueous activating solution comprising sulfuric acid or a strong acid derivative of sulfuric acid having a concentration of 75 to 85 percent by weight and a surfactant for a time period and temperature sufficient to render said surfaces water-wettable but 15 less than that wherein substantial mechanical degradation of said monofilament occurs.
• the present invention also provides a process for completely and substantially uniformly coating the surface of a polymeric monofilament with an electrically conductive electroless nickel coating wherein said surface is 20 modified by the process of contacting the monofilament with acid and surfactant solution prior to coating with said nickel characterized by feeding said monofilament from at least one feed reel, through an electroless nickel bath to at least one take-up reel wherein tension on said monofilament within said bath is sufficiently low to permit complete and substantially uniform 25 coating.
• the invention includes monofilaments and yams of monofilaments coated with electrically conductive nickel-boron alloy coatings.
• FIG. 30 The figure shows an apparatus suitable for processing yarn in accordance with this invention.
• the surfaces of monofilaments in a yam to be coated with metal are contacted with an aqueous activating solution which renders the surfaces hydrophilic and facilitates adsorption of a catalyst for effecting electroless nickel deposition.
• the aqueous activating solution comprises an acid such as sulfuric acid, or a strong acid derivative of sulfuric acid such as methane- sulfonic acid, chlorosulfonic acid, fluorosulfonic acid, and the like and a surfactant having from 8 to 12 carbon atoms.
• Suitable surfactants include fiuoroalkyl salts, ethers and esters, polyethoxylated quaternary ammonium salts, sodium alkyl benzoates, polyethoxylated straight chain alcohols and the like.
• Particularly suitable surfactants include amine perflouroralkyl sulfonates, fluorinated alkyl alkoxylates, fluorinated alkylesters, fluorinated alkyl carboxylate salts or the like.
• the use of the surfactant permits using weaker acid compositions which permits longer contact times with the monofilament without substantial degradation. The increased permissible contact times permit increased penetration of the aqueous activating composition into interior monofilaments of any yam being treated.
• the yam or monofilament surfaces then are contacted with a palladium catalyst in order to provide a catalytic surface for the electroless deposition of electrically conductive metal.
• nickel as it relates to the electrolessly-applied metal coating, refers to a nickel/boron alloy and excludes nickel/phosphorous alloys.
• the electroless nickel bath contains both nickel and boron and a reducing agent which produces the nickel-boron alloy coating for the polymeric monofilaments.
• monofilaments to be metal coated are passed, generally as yam, through an electroless bath to coat nickel completely and substantially uniformly on all the monofilament surfaces.
• Tension on the yam passing through the electroless nickel bath is either eliminated or maintained sufficiently low so that the nickel coatingsolution can penetrate into and through the entire yam bundle, in particular even on the surface of monofilaments located within the yarn bundle interior. It has been found that when the yam is passed through the electroless nickel bath under moderate significant tension, , the monofilaments at the interior of the yam bundle are either not coated at all or are incompletely coated so that the metal coating on the monofilaments is not uniform.
• the nickel coated yam can be coated electrolytically with an electrolytic metal such as copper or nickel.
• the electrolytic metal deposition also can be effected in a reel to reel process wherein the nickel-coated yam positioned within an agitated electrolytic aqueous bath is subjected to little or no tension to permit the aqueous electrolytic bath to penetrate into the interior of the yarn to be coated.
• the nickel coated or nickel and electrolytic metal coated monofilament or yam which can be braided or woven, functions as a substitute for metal wire.
• a virtually pure nickel substrate ( 1 ) is metallurgically compatible with a subsequent electrolytically applied layer of metal such as copper,
• electrolytically-deposited metal e.g. copper over the amine-borane nickel layer that, by reason of its dense fine-grained composition, (a) has excellent ductility and flexural endurance properties, (b) is more conductive per unit weight than electroless copper.
• a construction consisting of a yam bundle of polyaramid monofilaments metalized with amine-borane reduced electroless nickel only.
• metalized fibers find utility as conductive fillers which minimize electrostatic buildup on the surface of molded plastic parts used in electrical/electronic applications.
• the idealized metal coating must be bonded to the polyaramid monofilament surfaces with sufficient adhesion to withstand the mechanical abrasion of the chopping as well as the elevated temperature experienced in the injection molding processes, while at the same time providing an acceptable level of conductivity which does not materially change due to oxidation, unlike nickel-phosphorous alloy in the 10-20 ohm/foot range.
• the monofilament surfaces to be treated in accordance with this invention are formed from a polymeric compositions rendered more hydrophilic by the acid and surfactant activating solution to enable a more complete and more uniform electroless nickel coating on all the monofilament surfaces which is adherent and sufficiently electrically conductive to facilitate subsequent electrolytic metal coating on the conductive nickel.
• Suitable polymeric compositions for forming the monofilament or yam include aramid, such as poly(p-phenylene terephthalamide), poly (m-phenylene isophthalamide), and the like, polyamide, such as nylon 6, nylon 66, and the like, polyester, polyimide, polyetherimide, acrylics, polytetrafluoroethylene and the like, preferably aramid since it provides excellent tensile strength per unit weight.
• yams have a denier between about 55 and 3,000 and more typically between about 55 and 600 with 10-15 micron diameter monofilaments.
• the monofilaments can be solid or hollow.
• a surfactant permits using a weaker acid which results in reduced degradation to the monofilament surfaces
• sulfuric acid used in combination with a surfactant 75 to 85%, preferably 78 to 83% sulfuric acid can be utilized which permits increasing the contact time of the yam with the activating composition considerably while avoiding undesirable monofilament degradation.
• the increased contact time and the presence of a surfactant provides more complete penetration of the activating solution into the yam and thereby permits greater assurance of subsequent complete and substantially uniform electroless metal coating.
• the surfactant is utilized in concentration between about 10 and 1000 parts per million (ppm) preferably between about 100 and 500 ppm of the activating solution.
• acceptable nickel coated monofilaments can be made by treating the monofilaments with solutions known to improve the water wettability of surfaces such as potassium hydroxide, sodium hydroxide, or other caustic compositions used alone or in combination with a lower alcohol such methanol or ethanol, or chromic acid, or the like.
• the monofilaments can, also, be treated by immersion in 5 concentrated sulfuric acid as described in U.S. Patent 5,302,415, such as, for example, by immersion in 80 to 90 weight percent sulfuric acid, for 2 to 60 seconds at 10 to 100°C, although the fibers may be somewhat degraded by such immersion.
• the surfaces are contacted with any one of the catalyst systems well known to those versed in the art of electroless plating to effect electroless metal deposition.
• Catalyst combinations which can be used in conjunction with the sensitized surfaces are disclosed in U.S. Pat. Nos. 3,011,920 and 3,562,038
• the catalyst application is provided for a period, generally of one to about 5 five minutes, and then the sample is immersed in an acidic solution to remove tin from the surface in the process referred to as acceleration.
• the sample is then passed through in an electroless nickel bath for a period ranging from about two to ten minutes to provide the desired thickness of nickel.
• Deposition and activation of the catalyst and subsequent deposition 0 of the electroless nickel is conducted with the yarn under tension which is zero or is sufficiently low so that the treatment baths contact all the monofilament surfaces.
• a storage roll 10 has wound upon it multifilament yarns, 12 and 14.
• Guide rollers 16 and 18 pull yarns 14 and 12 5 from storage roll 10 and deposit the yams within bath 20 and onto endless web 22.
• Endless web 22 is moved about rollers 24 and 26, at least one of which is powered.
• Yams 12 and 14 are passed under guide rollers 28 and 30 and are removed from bath 20 by powered rollers 32 and 34 as treated yam 36 and 38.
• the bath can be the pretreatment bath, the catalyst deposition or 0 activation bath or the electroless nickel bath described above.
• Powered rollers 32 and 34 and the endless web 22 are operated at a speed to assure little or no tension on the yams 40 and 42 deposited in the bath 20 on endless web 22.
• Suitable electroless nickel baths are those which are boron-based rather than phosphorous based since the boron based baths deposit a form of nickel resistant to oxidation and which are sufficiently conductive to facilitate subsequent electrolytic metal deposition, such as copper onto the nickel surface.
• Suitable boron based electroless nickel baths are disclosed in U S
• Nickel Chloride NiCl 2 6H 2 0
• Dimethylamine Borane 3.0 g/1
• Nickel is deposited on the receptive surfaces by electroless
• 25 alloy is between about 8 and 15 micro-ohm cm.
• a typical specific resistivity of nickel-low phosphorous alloy is 20-50 micro-ohm cm; and for a nickel- high phosphorous alloy between 150-250 micro-ohm cm.
• the electroless layer is sufficiently thick to permit subsequent electrolytic deposition of a uniform metal layer such as copper. Generally, the electroless nickel layer is
• the nickel coated monofilaments can be further coated with electrolytic metal such as electrolytic copper in an electrolytic plating process step.
• electrolytic metal such as electrolytic copper
• the nickel coated yam is passed through an electrolytic plating bath under little or no tension so that
• the aqueous electrolytic plating bath can penetrate into the entire yam to contact all nickel coated monofilament surfaces.
• An electrical charge is applied to the electrolytic plating bath to effect electrolytic metal deposition completely and substantially uniformly on all nickel surfaces.
• the thickness of the electrolytic metal coating can be controlled by controlling the time,
• EXAMPLE 1 Para-aramid yarn of 200 denier(d) with 89 monofilaments was treated for 90 seconds in an aqueous activating solution of 79% sulfuric acid which contained 50 ppm of a 3: 1 mixture of a perfluorinated alkyl ester surfactant and a perfluorinated alkyl alkoxylate surfactant at 40°C.
• the para- aramid yam was a product sold by E. I. du Pont de Nemours and Company under the tradename "Kevlar”. The yam was then rinsed with water and conveyed through a continuous treating process under zero or very low tension on a carrier film as shown in the figure.
• the continuous process included a series of steps in a series of devices as shown in the figure with solutions which provided the catalyst system prior to electroless nickel deposition, final rinse, drying, and wind-up steps.
• the yam first passed through a solution which was about 5% NaOH which rendered the monofilament surfaces alkaline prior to passing into a palladium activating solution which was an ionic soluble palladium complex sold by Atotech, Inc. under the trade name, Neoganth 834.
• This solution was made up by using 3% of the Neoganth 834 palladium activator concentrate in 96.5% by volume deionized water with 0.5% of 50% NaOH solution used to adjust the pH to 11.5.
• the bath was heated to 50°C for about 2 hours and was then cooled to 45°C for use in treating the yam.
• the yam was passed through two rinse stations, each providing about 1 minute rinse with deionized water, then into a dimethylamineborane reducer solution sold by
• Atotech, Inc. under the tradename "Neoganth WA.
• the reducer solution was made by taking 0.5% by volume of the Neoganth WA concentrate and diluting it with 99% deionized water containing 0.5% boric acid as a pH buffer. This solution was heated to 35°C for use in reducing the soluble palladium ion to the palladium metal which provides active catalytic sites on the polymer surface to initiate electroless nickel deposition.
• the yam was conveyed directly from the reducer solution into an electroless nickel plating bath comprising Niklad 752, available from MacDermid Corp.
• This bath was operated at 70°C with a pH of 6.6 and contained dimethylamine borane as the reducing agent; and was made up according to the supplier's instructions for the desired percent of nickel and reducer.
• the yam was conveyed through the bath while supported on a carrier film under very low tension. Using high agitation in the bath, it was possible to obtain complete penetration of the bath into the yam bundle and uniform metalization of each monofilament. Typically, a 4 minute dwell time in this bath provided about 30% weight increase to the yarn by the nickel coating.
• the resultant coated yarn had a resistance of about 100 ohms/ft.
• Additional yams processed with 5 shorter dwell times provided proportionately less nickel and higher resistances, while longer dwell times provided proportionately higher metal addition with lower resistance.
• a cross-sectional analysis provided revealed complete and uniform deposition of nickel around all of the monofilaments in the yarn bundle.
• EXAMPLE 2 A hollow picture frame type rack was cut out of 1/1 6" polyethylene sheeting and U-shaped grooves were milled on the top and bottom of the rack so that yam could be wound around the rack loosely
• Niklad 797B sodium hypophosphite solution
• the pH was adjusted to 5.0-5.2 with 50% ammonia and the solution was heated to 90°C prior to immersion of the rack containing the yam sample.
• the racks were agitated
• the final dried yam had a resistance of 300 ohms/ft. which was three times higher than the coated yarn of Example 1.
• Examples 1 and 2 were repeated except that the yams were treated in concentrated sulfuric acid for a much shorter time as taught in U.S. Patent 5,302,415. To minimize substantial degradation of the monofilaments. it was necessary to limit the immersion of the yams in the concentrated sulfuric acid to only half as long as the immersions of Examples 1 and 2.
• the coated yarns exhibited electrical resistances similar to the coated yams of Examples 1 and 2.
• EXAMPLE 5 The metalized yam obtained by the process of Example 1 was subsequently electroplated with copper by passing the nickel coated yam through a gas agitated electrolytic acid copper sulfate plating bath fitted with contact bars which passed electrical current into the yam as it entered and exited from the plating bath.
• the nickel coated yam could withstand about 5 amps of current before sustaining yam damage and added about 65% by weight of copper to produce a material that had a resistance less than 1 ohm/ft.
• This copper plated yam still retained all of the good handling, drape, and flexibility characteristics of the original starting yam.
• This electrolytic plating provided a fine grained equi-axial crystal structure on the copper.

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• Materials Engineering (AREA)
• Mechanical Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Textile Engineering (AREA)
• Inorganic Chemistry (AREA)
• Chemical Or Physical Treatment Of Fibers (AREA)
• Chemically Coating (AREA)

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• 1997
  • 1997-05-30 CA CA002255646A patent/CA2255646C/en not_active Expired - Lifetime
  • 1997-05-30 JP JP50299398A patent/JP4060363B2/ja not_active Expired - Lifetime
  • 1997-05-30 WO PCT/US1997/009116 patent/WO1997048832A2/en not_active Ceased
  • 1997-05-30 DE DE69709094T patent/DE69709094T2/de not_active Expired - Lifetime
  • 1997-05-30 EP EP97944281A patent/EP0902854B1/de not_active Expired - Lifetime
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